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Mid-diaphyseal Endosteal Thickening With Subsequent Medullary Narrowing in a Patient With Hallermann-Streiff Syndrome

We report on a 5-year-old girl who presented with the full clinical criteria of Hallermann-Streiff syndrome (HSS). Classically, overtubulation (thin and gracile) bones are the characteristic and constant features in HSS. Interestingly, our present patient manifested unusual mid-diaphyseal endosteal...

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Autori principali: Kaissi, Ali Al, Handelbauer, Albert, Klaushofer, Klaus, Grill, Franz
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elmer Press 2011
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3279479/
https://ncbi.nlm.nih.gov/pubmed/22393346
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4021/jocmr704e
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